Manuela Pendziwiat
Impact in
- Psychiatry and Mental health top 1%
- Epilepsy research and treatment
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Papers in
-
- Epilepsy research and treatment 42
- Genetics 17
- Genomics and Rare Diseases 10
- Genetics and Neurodevelopmental Disorders 8
- Co-authors
- Gregor Kuhlenbäumer (10 shared papers)Ingo Helbig (13 shared papers)Zaid Afawi (8 shared papers)Silke Appenzeller (6 shared papers)Charles Vaughn Sindelar (1 shared paper)Xiaobo Bai (1 shared paper)Kaifeng Zhou (1 shared paper)Elias T. Spiliotis (1 shared paper)
- Journals
- The American Journal of Human Genetics (10 papers)Epilepsia (7 papers)Neurology (6 papers)Brain (4 papers)Movement Disorders (3 papers)
- Partner nations
- GermanyUnited StatesFrance
In The Last Decade
Manuela Pendziwiat
65 papers receiving 2.8k citations
Manuela Pendziwiat's Hit Papers
Peers
Comparison fields: 5 of 87
- Psychiatry and Mental health 1.4k
- Clinical Biochemistry 139
- Genetics 738
- Neurology 196
- Cellular and Molecular Neuroscience 192
Countries citing papers authored by Manuela Pendziwiat
This map shows the geographic impact of Manuela Pendziwiat's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Manuela Pendziwiat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuela Pendziwiat more than expected).
Fields of papers citing papers by Manuela Pendziwiat
This network shows the impact of papers produced by Manuela Pendziwiat. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Manuela Pendziwiat. The network helps show where Manuela Pendziwiat may publish in the future.
Co-authors
The 25 scholars most cited alongside Manuela Pendziwiat, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 223 | |
| 2 | 2018 | 214 | |
| 3 | GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Hit paper breakdown → | 2023 | 129 |
| 4 | 2015 | 121 | |
| 5 | 2018 | 116 | |
| 6 | 2019 | 106 | |
| 7 | 2017 | 97 | |
| 8 | 2021 | 95 | |
| 9 | 2013 | 92 | |
| 10 | 2017 | 89 | |
| 11 | 2019 | 86 | |
| 12 | 2015 | 84 | |
| 13 | 2017 | 84 | |
| 14 | 2018 | 79 | |
| 15 | 2016 | 75 | |
| 16 | 2018 | 74 | |
| 17 | 2016 | 72 | |
| 18 | 2019 | 63 | |
| 19 | 2020 | 58 | |
| 20 | 2018 | 55 |
About Manuela Pendziwiat
Manuela Pendziwiat is a scholar working on Psychiatry and Mental health, Genetics, Neurology, Clinical Biochemistry and Rheumatology, having authored 65 papers that have together received 2.9k indexed citations. Recurring topics across this work include Epilepsy research and treatment (42 papers), Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (8 papers), Metabolism and Genetic Disorders (5 papers), Glycogen Storage Diseases and Myoclonus (5 papers), Neurological disorders and treatments (5 papers), Parkinson's Disease Mechanisms and Treatments (5 papers) and Lysosomal Storage Disorders Research (3 papers). The work is most often cited by research in Psychiatry and Mental health (1.4k citations), Clinical Biochemistry (139 citations), Genetics (738 citations), Neurology (196 citations) and Cellular and Molecular Neuroscience (192 citations). Manuela Pendziwiat has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Gregor Kuhlenbäumer, Ingo Helbig, Zaid Afawi, Silke Appenzeller, Charles Vaughn Sindelar, Xiaobo Bai, Kaifeng Zhou, Elias T. Spiliotis, Amos D. Korczyn and Hadassa Goldberg‐Stern. Their work appears in journals such as The American Journal of Human Genetics, Epilepsia, Neurology, Brain and Movement Disorders.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.